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European Journal of Medical Genetics|February 11, 2018
ZNF462 and KLF12 are disrupted by a de novo translocation in a patient with syndromic intellectual disability and autism spectrum disorderNele Cosemans, Laura Vandenhove, Jarymke Maljaars, et al.Developmental Medicine and Child Neurology|March 16, 2007
Motor development in school-aged children with 22q11 deletion (velocardiofacial/DiGeorge syndrome)Katrijn Van Aken, Bert De Smedt, Annelies Van Roie, et al.European Journal of Human Genetics : EJHG|November 4, 2004
A further mutation of the FGFR2 tyrosine kinase domain in mild Crouzon syndromeThomy J L de Ravel, Indira B Taylor, Alex J T Van Oostveldt, et al.Clinical Dysmorphology|January 7, 2003
Familial cryptic translocation with deletion 4q33-->4qter and duplication 7q34-->7qter in brothers with mental retardation, macrocephaly and iris colobomaUte Moog, John J M Engelen, Henny M J van Schrojenstein Lantman-de Valk, et al.International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|July 29, 2016
Fertility Preservation Is Safe for Serous Borderline Ovarian TumorsEveline Vancraeynest, Philippe Moerman, Karin Leunen, et al.International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|June 3, 2017
Neoadjuvant Weekly Paclitaxel-Carboplatin Is Effective in Stage I-II Cervical CancerRawand Salihi, Karin Leunen, Philippe Moerman, et al.Gynecologic and Obstetric Investigation|July 10, 2017
Staging with Unilateral Salpingo-Oophorectomy and Expert Pathological Review Result in No Recurrences in a Series of 81 Intestinal-Type Mucinous Borderline Ovarian TumorsKobe Dewilde, Philippe Moerman, Karin Leunen, et al.Gynecologic Oncology|June 25, 2003
The diagnostic problem of endometrial stromal sarcoma: report on six casesFrédéric Amant, Philippe Moerman, Isabelle Cadron, et al.American Journal of Ophthalmology|March 1, 2011
High frequency of submicroscopic chromosomal deletions in patients with idiopathic congenital eye malformationsIrina Balikova, Thomy de Ravel, Carmen Ayuso, et al.Journal of Investigative Medicine : the Official Publication of the American Federation for Clinical Research|December 13, 2006
Focal segmental glomerulosclerosis in patients with mandibuloacral dysplasia owing to ZMPSTE24 deficiencyAnil K Agarwal, Xin J Zhou, Roger K Hall, et al.Pageof 25